StompOnStep1.com a. Assume this pedigree represents inheritance of a human disease. What is the most likely mode of inheritance for this disease? b. What is the most likely genotype person III-IV if we use A and a as the alleles for this disease? a. Autosomal dominant, b. Aa a. Y linked, b. Aa a. Autosomal dominant, b. AA a. Autosomal recessive, b. aa

StompOnStep1.com a. Assume this pedigree represents inheritance of a human disease. What is the most likely mode of inheritance for this disease? b. What is the most likely genotype person III-IV if we use A and a as the alleles for this disease? a. Autosomal dominant, b. Aa a. Y linked, b. Aa a. Autosomal dominant, b. AA a. Autosomal recessive, b. aa

Name: O StompOnStep1.coma. Assume this pedigree represents inheritance of a
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Description: O StompOnStep1.coma. Assume this pedigree represents inheritance of a human disease.What is the most likely mode of inheritance for this disease?b. What is the most likely genotype person III-IV if we use A and a asthe alleles for this disease?a. Au

Biology (MindTap Course List)

11th Edition

ISBN:9781337392938

Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Publisher:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Chapter16: Human Genetics And The Human Genome

Section: Chapter Questions

Problem 10TYU: Examine the following pedigrees. Which is the most likely mode of inheritance of each disorder? (a)...

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Retinitis pigmentosa, a form of blindness in man, maybe caused either by a dominant autosomal gene R, or a recessive autosomal gene a. An afflicted man whose parents are both normal marries a woman with genotype AaRr. a. What proportion of the children are expected to suffer from this affliction if R and A are inherited independently? b. If this couple want to have normal children only, what isthe probability of having normal children?
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Complete the following queatione BEFORE ATTEMPTING THE HW 1 BLACKBOARD ASSIGNMENT, In the following human pedigrees, the filled symbols represnent the affected individuals who suffer from the disease. Use A/a to represent alleles for autosomal traits and XIX/Ytorepresent alleles for X-linked traits. Use the uppercase letter to represent the dominant allele and the lowercase letterto represent the receasive allele. afected fomale Unafected female affected male Unaffected male Pedigree 1: A. What is the most likely mode of inheritance of this disease? Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive. B. State the genotypes of individuals #1-#3. C. What is the probability that individual #4 is a carrier of this disease if his mother is homozygous dominant and his father is heterozygous? Pedigree 2: What is the most likely mode of inhentance of this disease? Choose from: autosomal dominant, autosomal recessive X-linked dominant X-linked recessive.…
Could the characteristic followed in the pedigree be caused by an autosomal dominant disease? Why or why not? 3 4. O No, the offspring of 1-3 and I-4 contradict an autosomal dominant inheritance O No. the offspring of 1-1 and I-2 contradict an autosomal dominant inheritance O Yes, all individuals fit the autosomal dominant inheritance pattern ONo, the offspring of II-3 and -4 contradict an autosomal dominant inheritance
Shaded in black-white trait (Glucose-6-phosphate dehydrogenase deficiency) 1. What type of x-linked inheritance is shown in the chart above? a. X-linked Dominant b. X-linked Recessive c. Autosomal Dominance d. Autosomal Recessive 2. What is the genotype of individual 1 at generation I? a. XGXG b. XGXg c. XX d. XO
re ||| E 6. Label the genotypes for this pedigree of an X-linked recessive disorder (red- green colorblindness). (a) 2 2 3 1 3 a. How do you know? b. Label the genotypes. 4 O To 2 4 5 5 6 6 7. Is the following pedigree autosomal recessive, autosomal dominant or X-linked recessive? 2 8 O T 58
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III. For each of these three pedigrees, determine the likely mode of inheritance and the probability that individual will express the trait. A. B. I C. III || IV Mode of inheritance I || IV Mode of inheritance I || O III 04-0 오ㅜㅁ 오ㅜㅁㅇㅁ IV O Mode of inheritance = O P() expresses trait = P() expresses trait = OD P() expresses trait =
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While studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this sign was founded only in the men and it was inherited from father to the son. Define the type of hypertrichosis inheritance? Select one: a. Y-linked b. Autosomal-recessive O c. Autosomal-dominant d. Recessive, X-linked e. Dominant, X-linked
Figure 16.4 Two common patterns of autosomal inheritance in humans. & Both parents are heterozygous. b. One parent is heterozygous, and the other is homozygous recessive. The alleles stands for any trait that is dominant, and the letter a stands for any trait that is recessive Substitute the correct alleles for the problems you are working on. For example, C normal, c- cystic fibrosis Parents d 9 A A An X eggs Offspring m Key Dominant allele Recessive allele Dominant phenotype Recessive phenotype Phenotypic Ratio words A a Parents AT X Ag 40 eggs Offspring an A An an Key A Dominant allele Recessive allele Dominant phenotype Recessive phenotype Phenotypic Ratio Autosomal Disorders 1. Neurofibromatosis (NF), sometimes called von Recklinghausen disease, is one of the most common genetic disorders. It affects roughly 1 in 3,000 people. At birth or later, the affected individual may have six or more large, tan spots on the skin. Such spots may increase in size and number and become darker.…